Concepedia

Author

Maurice Godfrey

University of Nebraska Medical Center

Also Known As

M D Godfrey, M GODFREY, M Godfrey, M. Godfrey, MAURICE GODFREY, Maurice Godfrey

88

Publications

5.5K

Citations

32

H-Index

91

Concepts

All Affiliations

University of Nebraska Medical CenterNebraska Medical CenterOregon Health & Science UniversityColumbia UniversityCenter for Human Genetics
MG

About

Maurice Godfrey is an author at University of Nebraska Medical Center specializing in medicine, molecular genetics, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

17

22

3K

2

Public Health

3

3

791

3

Engineering

2

2

36

4

Natural Sciences

1

1

154

5

Anatomy

1

1

14

Maurice Godfrey

×

42

Publications

4.9K

Citations

30

H-Index

YearCitations

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

Brendan Lee, Maurice Godfrey, Emilia Vitale,

Nature

1991

671

The isolation and nucleotide sequence of a cDNA encoding the T cell surface protein T4: a new member of the immunoglobulin gene family

Paul J. Maddon, Dan R. Littman, Maurice Godfrey,

Cell

1985

664

Immunohistologic Abnormalities of the Microfibrillar-Fiber System in the Marfan Syndrome

David W. Hollister, Maurice Godfrey, Lynn Y. Sakai,

New England Journal of Medicine

1990

395

Functional interaction between human T-cell protein CD4 and the major histocompatibility complex HLA-DR antigen

Denise Gay, Paul J. Maddon, Rafick‐Pierre Sékaly,

Nature

1987

348

Autocrine Role of Interleukin-8 in Induction of Endothelial Cell Proliferation, Survival, Migration and MMP-2 Production and Angiogenesis

Aihua Li, Michelle L. Varney, Jason Valasek,

Angiogenesis

2005

285

In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome: Figure 1

Laurence Faivre, Robert J. Gorlin, Mary K. Wirtz,

Journal of Medical Genetics

2003

280

Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly to the Fibrillin Genes on Chromosomes 15 and 5

Petros Tsipouras, R. Del Mastro, M. Sarfarazi,

New England Journal of Medicine

1992

273

Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40

Frank Tiecke, Stefanie Katzke, Patrick Booms,

European Journal of Human Genetics

2001

157

Glycine to serine substitution in the triple helical domain of pro-α 1 (II) collagen results in a lethal perinatal form of short-limbed dwarfism

Henrik Vissing, Marina D’Alessio, B Lee,

Journal of Biological Chemistry

1989

154

Structure and expression of the human and mouse T4 genes.

Paul J. Maddon, Susan M. Molineaux, D.E. Maddon,

Proceedings of the National Academy of Sciences

1987

152

Page 1